This category contains 32 nodes.
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features.
This node can be used to merge statistics of the featureCounts node.
Tools to manipulate SAM/BAM files
Pindel - a pattern growth approach to detect breakpoints of large deletions and medium sized insertions from paired-end reads.
This node sorts the chromosomes of an input VCF file analogous to a given reference sequence.
This node filters annotated VCF files.
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